Researcher Job at Norstella | Medical Remote Jobs – Apply Now
Looking for a rewarding researcher job in the life sciences industry? Explore an exciting opportunity with Norstella, offering one of the most promising medical remote jobs in India. This role supports cutting-edge drug intelligence and AI-driven insights that accelerate patient access to life-saving therapies. If you’re seeking growth through Norstella careers, this full-time remote position could be your next big step.
Job Details:
- Job Title: Researcher, Drugs
- Company: Norstella
- Location: Remote, India
- Date Posted: Feb 16, 2026
- Employment Type: Full Time
- Job ID: R-1723
About the Company
Norstella is a premier and critical global life sciences data and AI solutions provider dedicated to improving patient access to life-saving therapies. Norstella supports pharmaceutical and biotech companies across the full drug development lifecycle – from pipeline to patient. The mission is simple: to help clients bring therapies to market faster and more efficiently, ultimately impacting patient lives. Professionals exploring Norstella careers and high-impact medical remote jobs will find this researcher job aligned with innovation and global healthcare transformation.
Job Description
The Researcher supports the creation of high-quality drug intelligence content by conducting structured secondary research, extracting regulatory and clinical information, and ensuring data integrity. This researcher job plays a key part in developing reliable pharma R&D content for Norstella’s platforms, contributing to our mission of accelerating access to life-saving therapies. This opportunity is ideal for professionals seeking medical remote jobs that combine regulatory knowledge, therapeutic expertise, and data-driven research within growing Norstella careers.
Qualifications
- Graduate/Post-Graduate/Doctorate degree in Medical Sciences, or a related discipline
- Minimum 1 year of experience in pharmaceutical research, clinical data, or drug content development preferred
- Understanding of regulatory databases (e.g., ClinicalTrials.gov, EMA, FDA) and public data sources
- Familiarity with drug development lifecycle, therapeutic areas, and MoAs
- Proficient in MS Office Suite, especially Excel and Word
Key Responsibilities
- Identify and extract key drug data from public sources (e.g., clinical trial registries, regulatory filings, company reports)
- Demonstrate working knowledge of FDA, EMA, and other global regulatory agencies’ processes
- Apply foundational knowledge of therapeutic areas and mechanisms of action (MoAs) to drug research
- Adhere to SOPs and gather information from source publishing processes.
- Check and validate content for accuracy and basic errors before submission
- Meet daily and weekly productivity targets while ensuring data quality
- Develop proficiency in authoring tools and extensions to support publishing
